Vacuum battery system for portable microfluidic pumping

ABSTRACT

A fluidic chip employing a vacuum void to store vacuum potential for controlled micro-fluidic pumping in conjunction with biomimetic vacuum lungs.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a 35 U.S.C. §111(a) continuation of PCTinternational application number PCT/US2015/050595 filed on Sep. 17,2015, incorporated herein by reference in its entirety, which claimspriority to, and the benefit of, U.S. provisional patent applicationSer. No. 62/051,678 filed on Sep. 17, 2014, incorporated herein byreference in its entirety. Priority is claimed to each of the foregoingapplications.

The above-referenced PCT international application was published as PCTInternational Publication No. WO 2016/044532 on Mar. 24, 2016, whichpublication is incorporated herein by reference in its entirety.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not Applicable

INCORPORATION-BY-REFERENCE OF COMPUTER PROGRAM APPENDIX

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NOTICE OF MATERIAL SUBJECT TO COPYRIGHT PROTECTION

A portion of the material in this patent document is subject tocopyright protection under the copyright laws of the United States andof other countries. The owner of the copyright rights has no objectionto the facsimile reproduction by anyone of the patent document or thepatent disclosure, as it appears in the United States Patent andTrademark Office publicly available file or records, but otherwisereserves all copyright rights whatsoever. The copyright owner does nothereby waive any of its rights to have this patent document maintainedin secrecy, including without limitation its rights pursuant to 37C.F.R. §1.14.

BACKGROUND

1. Technical Field

This description pertains generally to diagnostic sensing systems, andmore particularly to passive diagnostic sensing systems.

2. Background Discussion

Low cost, power-free, portable, and controlled microfluidic pumping arecritical traits needed for next generation disposable point-of-caremedical diagnostic chips. Ideally, the pumping system should enabledisposable chips to perform on-site testing, where there may be poorinfrastructure (i.e. trained technicians, power source, or equipment).Furthermore, the pumping system should provide a platform that iscompatible with common quantitative analysis techniques that are usuallydone in centralized labs such as the Enzyme-Linked Immunosorbent Assay(ELISA) or Polymerase Chain Reaction (PCR). Preferably, the pumpingsystem should also have good optical characteristics so various types ofoptical detection can be utilized. Finally, it should be simple androbust enough so it can be operated with minimal or no training.

Microfluidic pumping is basically a method to drive fluid flow inminiaturized fluidic systems. Microfluidic pumping can generally bedivided into two main categories: active or passive pumping, dependingon whether the pumping uses external power sources. Active pumpingexamples include syringe pumps, peristaltic pumps, membrane basedpneumatic valves, centrifugal pumps, electro-wetting on dielectrics(EWOD), electrosmosis, piezoelectric pumps, and surface acoustic waveactuation methods. Typically active pumping systems have more preciseflow control and generally larger flow volumes compared to passivesystems. However, the requirement of external power sources, peripheralcontrol systems, or mechanical parts makes the devices more bulky,complex, or costly. These barriers make active pumping systems far lessfeasible for low cost disposable point-of-care systems.

In passive pumping, there are two main types: capillary or degaspumping. These two types are termed passive because these systemstypically do not require power sources or peripheral equipment forpumping, thus they are ideal for low cost point-of-care assays. Forcapillary systems, the lateral flow assay (e.g. pregnancy dipsticktests) is a prevalent commercial example. These assays use fibrousmaterials to wick bodily fluids in for immunoassays. However, the opaqueor reflective fibers can obstruct optical path, or cause higherbackground noise in fluorescent detection. These reasons maketransmission type optical detection, such as fluorescence, phasecontrast, and dark-field microscopy difficult to perform in papercapillary formats.

There is also capillary pumping in plastic formats. Glucose test stripsare a very common commercial example of this category. These test stripswick blood into a plastic slit for electrochemical detection. However,since capillary force is dependent on geometry, there are intrinsiclimitations in design. For example, channels cannot be too thick, andtherefore deep (mm scale) optically clear wells with large diameters arenot compatible with capillary designs. Flow channels also cannot be toowide, as bubbles may be easily trapped. Periodic structures have beenused to prevent bubbles from being trapped, but these structures makethe fluidic regions not flat and are less desirable for opticaldetection, as they can cause excessive scattering; for instance, indark-field microscopy or total internal reflection microscopy.Furthermore, special surface treatment steps are often needed to renderthe surfaces hydrophilic/hydrophobic, and flow speeds are highlysensitive to surface tension differences among liquids.

Finally, in all capillary formats, it is not possible to have completedead-end loading or post degassing to remove bubbles. Dead-end loadingis useful in nucleic acid amplification applications as it preventsevaporation. However, dead-end loading cannot be done in capillarysystems because an outlet vent for air is always necessary. Dead-endloading and the removal of bubbles are of critical importance ifelevated heat processes are involved, such as heat cycling during PCR,since bubbles can expand and cause a catastrophic expulsion of thefluids in the device.

With degas pumping, fluid flow is driven when air pockets diffuse intothe surrounding air permeable pre-vacuumed silicone materials, such aspolydimethylsiloxane (PDMS). It is analogous to a dry sponge soaking inwater, but instead of water, air is diffused into the vacuumed siliconeand draws fluid movement. The main advantages of degas loading are theability to load dead-end chambers, have great optical clarity, and allowfor more flexibility in design geometries, as deep and wide structurescan be loaded without air bubbles. However, the main drawback is thelack of flow control, and fast exponential decay of flow rate when thedevice is taken out of vacuum.

BRIEF SUMMARY

The present description includes a medical diagnostic assay with aportable and low cost pumping scheme employing a vacuum battery system,which pre-stores vacuum potential in a void vacuum battery chamber, anddischarges the vacuum over gas permeable lung-like structures to driveflow more precisely.

Another aspect is a fluidic chip employing a vacuum void to store vacuumpotential for controlled fluidic pumping in conjunction with biomimeticvacuum lungs. The chip exhibits significant advancements in four keyareas of flow control compared to conventional degas pumping for usewith digital amplification assays, including: more reliable and stableflow, with about 8 times less deviation in loading time and up to about5 times increase of the decay time constant for a much slower and stableexponential decay in flow rate; reliable pumping for up to about 2 hourswithout any external power sources or extra peripheral equipment;increased loading speed to up to about 10 times, with a large loadingcapacity of at least 140 μl; tuning flow and increase flow consistencyby varying the vacuum battery volume or vacuum lung surface area.

In one embodiment, the pumping system of the present invention isconfigured for one-step sample prep and digital amplification, anddemonstrated quantitative detection of pathogen DNA(Methicillin-Resistant Staphylococcus Aureus) directly from human wholeblood samples in one-step (from about 10 to about 10⁵ copies DNA/μl).

Further aspects of the technology will be brought out in the followingportions of the specification, wherein the detailed description is forthe purpose of fully disclosing preferred embodiments of the technologywithout placing limitations thereon.

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING(S)

The technology described herein will be more fully understood byreference to the following drawings which are for illustrative purposesonly:

FIG. 1 is perspective view of a medical diagnostic sensing systememploying vacuum battery pumping mechanism in accordance with thepresent description.

FIG. 2A shows a close-up view of the dead end wells and correspondinginter-digitated air channels in accordance with the present description.

FIG. 2B shows a schematic circuit diagram representative of the vacuumbattery system of the present description.

FIG. 3 shows a side-sectional view of the fluidic chip of FIG. 1.

FIG. 4A through FIG. 4C show side-views of a simplified schematicdiagram of the vacuum battery-based diagnostic sensing system duringcharging, storage and discharging operational phases, respectively.

FIG. 5A through FIG. 5C show perspective views of the vacuumbattery-based diagnostic sensing system during charging, storage anddischarging operational phases, respectively

FIG. 6A is a plot showing the effect on flow speed by varying the timegap between taking the device out of vacuum and loading between thesystem of the present description and a conventional degassing system.

FIG. 6B is a plot showing a comparison of the standard deviation ofloading time extracted from FIG. 6A.

FIG. 7A is a plot showing flow volume vs. time.

FIG. 7B is a plot showing battery volume vs. time needed to load.

FIG. 8A and FIG. 8B are showing close-up schematic diagrams of an 8-lungpair and 4-lung pair respectively,

FIG. 9A shows a plot of flow volume vs. time for varying numbers of lungpairs.

FIG. 9B shows a plot of loading time vs. numbers of lung pairs.

FIG. 10 is a plot of flow rate vs. elapsed time after loading forvarious lung pair quantities and bulk degassing.

FIG. 11 is a plot of the time constant of flow rate for various lungpair quantities and bulk degassing.

FIG. 12A through FIG. 12F show actual fluorescent images of thereactions (contrast adjusted) and the correlation with nucleic acidconcentration.

FIG. 13 is a plot of the average intensity of time, showing that theintensity of positive spots increases to a detectable level in 10minutes.

FIG. 14 is a pot showing the detection range of the vacuum batterysystem.

FIG. 15 shows a simplified 2-D diffusion model of a vacuum battery chipin accordance with the present description.

FIG. 16 shows the simulated pressure profile of the dashed line in FIG.15.

FIG. 17A is a plot showing the number of wells digitized over time forvarious lung configurations.

FIG. 17B is a plot showing the time needed to load all wells for variousbattery volumes.

FIG. 18A and FIG. 18B are plots illustrating the change in digitizationspeed by varying the loading time gap.

DETAILED DESCRIPTION

FIG. 1 illustrates a medical diagnostic sensing system 10 in the form ofa fluidic chip 12 using a vacuum battery configuration for controlledpumping without any external peripheral equipment. Compared to capillarypumping, the chip 12 provides dead-end loading and fewer designconstraints in geometry or surface energy. Dead-end loading can enablemultiplexed assays such as digital PCR to provide a simple, portable,and low cost technology is ideal for point-of-care diagnostic systems.For purposes of this description, the chip 12 (which may be implementedin microfluidic scales and scales beyond microfluidic applications) isshown in a configuration embodied for liquid samples. However, it willbe appreciated that the systems and methods disclosed herein may beimplemented on gaseous fluids in addition to liquids. Accordingly, theterm “fluid” or “fluidic” is broadly interpreted to mean both gasses andliquids. Furthermore, the term “chip” is broadly defined to mean adevice comprising one or more layers of material and/or components,which may or may not be planar in shape.

The chip 12 incorporates a vacuum battery system 18 that includes a mainvacuum battery 20 and vacuum lung 14. Vacuum battery system 18 usesvoids to pre-store vacuum potential and gradually discharges vacuum viaair diffusion through alveoli-like structures (air or vacuum channels24) of vacuum lung 14 to drive flow of fluid through fluid lines 16 andfluid channels 26. The vacuum battery 20 and vacuum lung 14 componentsare connected to each other, but not physically connected to nor influid communication with the fluid lines 16 or fluid channels 26. Asseen in FIG. 1 chip 12 comprises a bi-layer construction having an upperlayer 40 and lower layer 42. Layers 40 and 42 are shown opaque in FIG. 1for clarity.

In a preferred embodiment illustrated in FIG. 1, two vacuum batterycomponents are included on the chip 12 to serve different purposes. Themain vacuum battery 20 connects to the vacuum lung 14, and draws air infrom the fluid channel 26 via diffusion across the vacuum lung 14. Itpumps the main fluid flow that goes from the inlet 32 through fluidlines 16 into the optical window/waste reservoir 34 and the liquidchannels 26 from left to right. An auxiliary well-loading vacuum battery30 is connected to auxiliary vacuum lines or air channels 22 adjacent toand inter-digitating with the dead-end wells 28 (also seen in greaterdetail in FIG. 2A). As in the main battery system 20, the auxiliarywell-loading vacuum battery 30 is not physically connected to the fluidchannels 16, and instead only draws air in via diffusion across the thinPDMS wall 25 separating auxiliary channels 22 from wells 28, and assistsin making the dead-end well's 28 loading speed faster. It is alsoappreciated that the auxiliary well-loading battery 30 is optional sinceconventional degas pumping can still cause the wells 28 to be loaded,albeit at a slower speed.

Dead-end loading is especially useful for PCR reactions because itminimizes evaporation problems. Also, dead-end wells 28 can be useful indigital PCR applications, where one PCR reaction is partitioned andcompartmentalized into multiple smaller volumes of reactions, and eachchamber is run until saturation for a digital readout. On the otherhand, dead-end wells 28 are also useful for multiplexed reactions, forexample multiple diseases can be screened in different wells. However,dead-end wells would not be possible to load with capillary loading, andconventional degas pumping is slow. Accordingly, the vacuum batterysystem 10 is at a unique advantage by demonstrating about 2 times fasterdead-end loading (See FIG. 18A and FIG. 18B) compared to conventionaldegas pumping. Chip 12 as illustrated in FIG. 1 is configured with 224dead-end wells. However, this is representative of one possibleconfiguration for exemplary purposes, and it is appreciated that othergeometric configurations and sizing may be employed.

The vacuum lung 14 is configured to mimics lung alveoli gas exchange byallowing air to diffuse through thin gas-permeable silicone (e.g. PDMSor the like material) walls 25 (defined by inter-digitating air channels24 and fluid channels 26) from the fluid lines 16 into the vacuumbattery 20. It is important to note that the vacuum battery system 18 isnot connected to fluid lines 16 or channels 26, as vacuum would beinstantly lost once the device is taken out of a vacuum environment ifit was connected. Instead, the gas diffusion is controlled across airpermeable silicone material by design of the thin walls 25 to regulateflow properties.

The vacuum battery 20 and the vacuum lungs 14, individually, andparticularly in combination, greatly improve the pumping characteristicsof the system 10 compared to conventional bulk degas pumping in terms ofrobustness, speed, and operation time.

Firstly, the vacuum battery void 20 can provide more vacuum potentialstorage than bulk PDMS, and therefore more air can be outgassed andresulting in more liquid being sucked in. Since more vacuum isaccumulated, a longer operation time is possible. This is analogous tothe arranging batteries in parallel to discharge longer. FIG. 2Billustrates a simple circuit diagram of the battery potential via vacuumwith regard to the fluid resistance.

Secondly, since the main vacuum potential is stored in the vacuumbatteries 20, 30, instead of the bulk PDMS, the system 10 is lesssusceptible to losing vacuum power from the sides of the chip 12. Thiscontributes to the higher consistency of fluid loading.

Thirdly, air no longer has to diffuse through bulk PDMS material, butonly through a thin PDMS wall 25 (e.g. walls between air channels 24 andfluid channels 26 and between auxiliary air channels 22 and dead-endwells 28). This translates into faster and more consistent flow. Inconventional bulk degas diffusion, there is a characteristic initialsharp exponential drop in flow rate as air diffuses into the surfacelayers of PDMS, but becomes much slower afterwards as air takes muchlonger to diffuse into the bulk material. More consistent flow ispossible since vacuum diffuses with a more constant pressure drop acrossthe vacuum lung thin PDMS walls as the vacuum battery provides a largecapacitance for vacuum energy storage.

Fourthly, the flow rate can be easily tuned and increased by modifyingthe surface area of the vacuum lung 14 diffusion area (see FIG. 8A andFIG. 8B) or increasing the vacuum battery 20 volume. The combinedeffects of the vacuum battery system 18 plus bulk degas pumping alsohelp increase the flow rate.

Additionally, in contrast to capillary pumping, the vacuum batterysystem 10 enables more flexibility in the design of geometries. In oneexemplary configuration, a deep reservoir 34 (e.g. 5 mm diameter, 3 mmheight) to retain the excess of pumped liquid. This reservoir 34 enableslarge loading volumes of liquid to be continuously pumped in. The devicecan pump in at least 140 μl, and volume can be easily be furtherincreased by punching larger waste reservoirs and vacuum batteries. Thisis possible because the vacuum battery 20 significantly adds to thevacuum capacity of the device compared to bulk degassing systems. Thisadditional capacity is the driving force that helps outgas the remainingair volume. The reservoir 34 also helps prevent liquid from immediatelyflowing into the vacuum lung area 14, thus preventing the flow rate tobe affected prematurely when the liquid covers the surface area for gasdiffusion.

The capacity for a large and deep reservoir 34 is also advantageous forfluorescent or transmission type optical detection, as the Beer Lambartlaw can be fully utilized since the optical path length is longer. Forexample, Enzyme-Linked Immunosorbent Assays (ELISA), or real-time PCRassay are common examples that use transmission type optical detection,which can be benefit from system 10.

FIG. 3 shows a side-sectional view of the chip 12 of FIG. 1. Upper PDMSlayer 40 includes an aperture for inlet 32, and lower PDMS layer 42comprises reservoir 34, battery cavity 20, and channels for lungs 14 andfluid lines 16. Pressure sensitive adhesive layers 44 may be applied onboth the bottom and top surface of the chip 12 to prevent excess gasdiffusion.

FIG. 4A through FIG. 4C show side-views of a simplified schematicdiagram of the vacuum battery-based diagnostic sensing system 10 duringcharging, storage and discharging operational phases, respectively. FIG.5A through FIG. 5C show perspective views of the vacuum battery-baseddiagnostic sensing system 10 during charging, storage and dischargingoperational phases, respectively. As seen in FIG. 4A through FIG. 4C andFIG. 5A through FIG. 5C, there basically are three cycles for operationof the system, depicted as configurations 10 a, 10 b, and 10 c. Anoptional waste reservoir 34 is also shown in FIG. 4A through FIG. 4C andFIG. 5A through FIG. 5C. While the waste reservoir helps to increaseloading volume, although such reservoir is not necessary for operation.

The first cycle depicted in FIG. 4A and FIG. 5A is the charging phase,where the system 10 a is put in a vacuum environment and the air fromthe vacuum battery 20 slowly diffuses out through channels 24, acrossthe thin membranes 25 to the fluid channels 26, and eventually out inlet32. Air also degasses out of the bulk PDMS material from the sides ofthe chip 12. This step is generically termed as the “charging vacuumpotential” step.

In the second cycle depicted in FIG. 4B and FIG. 5B, the chip 12 ispacked with a vacuum-sealing machine in an air-tight seal orcontainment, e.g. an aluminum pouch 50 or like vacuum containment. Thisstep is primarily performed if long-term storage is needed. The chip 12can be stored indefinitely and transported easily in such vacuum pouch,which is desirable for point-of-care diagnostic devices. This step isgenerically termed as the “storage” step. No observable loading speeddifferences were found with devices that were stored in such pouches forup to a year.

In one embodiment, the chip 12 is incubated in vacuum overnight, andthen is sealed in aluminum pouch 50 with a vacuum sealer. A layer ofplastic may be laminated on the inside of the aluminum seals (notshown), such that sealing of the pouch 50 may be affected by heating theseams up to melt and seal the pouch 50.

In the third cycle depicted in FIG. 4C and FIG. 5C, the user simplyopens the pouch 50 and loads/applies the liquid sample 52 at inlet 32.The vacuum potential from battery 20 and lungs 14 pulls air from thefluid lines 26 across membranes 25 into lungs 24 and battery 20, thusadvancing the liquid sample 52 from the inlet 32 into optional reservoir34 and into fluid channels 26.

It should be noted that FIG. 4A through FIG. 5C are simplifiedillustrations, and the fluid sample 52 may also be directed throughfluid lines 16 and dead-end wells 28 via vacuum potential from auxiliaryreservoir 30 as shown in FIG. 1. The third step is generically termedthe “discharging” step, and is configured to be is simple andstraightforward, so no special training is required to perform it.

Example

The systems and methods of the present description were implemented in atest configuration similar to the system vacuum battery 10 embodied inFIG. 1, and the effects of the vacuum battery system 10 on flow rateswere compared with conventional degas pumping.

The tested fluidic chips 12 were fabricated using the standard softlithography process. A master mold with protruding microfluidic channelswas created by photo-patterning (e.g. OAI Series 200 Aligner) 300 μm ofSU-8 photoresist (e.g. Microchem) onto silicon wafers. Then 3 mm ofPolydimethylsiloxane (e.g. PDMS, Sylgard 184, Dow Corning) was pouredand cured over the silicon wafer mold to replicate the microfluidicchannels. All chips were made to the same size of 25 mm×75 mm by placinga laser cut acrylic cast around the silicone mold, which is the samefootprint as a standard microscope glass slide. The waste reservoir waspunched by a 5 mm punch. A separate blank piece of 3 mm PDMS would bebonded on the top side to seal the fluidic layer by oxygen plasmabonding. Finally, transparent pressure sensitive adhesives were taped onboth the bottom and top surface of the chip to prevent excess gasdiffusion.

The vacuum battery void 20 may be fabricated by simply punching the PDMSfluidic layer with through holes before bonding the top and bottom PDMSlayers. Different diameters of punchers would be used to fabricatedesired vacuum battery volumes. The pressure sensitive adhesive tapeused to cover the top and bottom sides may also seal the battery voidsinto compartments.

To generate the vacuum charge, the chips were incubated at −95 kPa for24 hours in a vacuum chamber before liquid loading experiments. Thechips were sealed in aluminum vacuum packs by a vacuum sealer iflong-term storage was necessary.

Parametric studies were performed by varying the operation time gaps,volume of vacuum battery, and surface area of the vacuum lung pairs.Results show that the vacuum battery system increases reliability of theflow, has longer loading windows, has faster loading, and is easy totune flow.

The effect of the time gap between releasing the chip from vacuum andloading liquids was tested to demonstrate that the vacuum system 10 ofthe present description provides a sufficient long window of operationso users can load the samples at reasonable times after opening thevacuum seal. A volume of 100 μl of blue food dye was loaded into theinlet 32 of the chip 12 at different time gaps after the chip 12 wastaken out of the vacuum. For purposes of this discussion, “digitization”is defined as being complete when all dead-end wells 28 of fluid lines16 are filled and compartmentalized when the air gap comes in (from leftto right in FIG. 1 prior to reaching reservoir 34). Furthermore, “fullyloaded” is defined as the point where liquid fills to the end of thevacuum lungs 14 (also from left to right toward the main battery well 20in FIG. 1).

A time-lapse comparison of actual loading between the vacuum batterysystem 10 of the present description and conventional degas pumpingsystem was performed. The front section of dead-end wells 28 wascompartmentalized to show adaptability for multiplexed reactions. Thechips 12 were loaded after being exposed to atmosphere for 10 minutesafter taking them out of vacuum. The vacuum battery system 10 finishedloading at 40 minutes, while the conventional degas pumping system stillhad significant portions that were not loaded.

Referring to the time gap and loading graph of FIG. 6A, it was alsofound that the vacuum battery system 10 was functional for a longerloading time gap for up to 40 minutes, whereas conventional degaspumping failed loading starting at 30 minutes. Even after idling inatmosphere for 40 minutes out of the vacuum, the vacuum battery system10 still remained functional and continued to pump for another 107minutes, thus it can be concluded that the vacuum battery system 10 canpump reliably for at least 2 hrs in total.

Though the conventional degas pumping method could continue to load forlonger times (e.g. about 50 to about 200 min, FIG. 6A) after the liquidis loaded into the inlet, the more important factor is the length of theinitial time gap that the user can load liquids in. Also, a longer postloading pumping time indicates that conventional degas pumping wasslower. It was found that regardless of the time gap, loading speed wasmuch faster in the vacuum battery system 10. For example, at 5 minutesafter releasing vacuum, the vacuum battery system 10 was 4.5 timesfaster in loading. Furthermore, the vacuum battery system 10 showed tobe much more robust, as it followed a linear trend nicely whileconventional degas had much more variation, with r² values at 0.97 and0.83, respectively.

FIG. 6B is a plot showing a comparison of the standard deviation ofloading time extracted from FIG. 6A. It was found that the vacuumbattery system 10 was much more consistent in repeatability, wherein thestandard deviation of the loading time of the vacuum battery system 10was about 8 times less in average than conventional degassing.

Experiments were also conducted to determine the effect of tuning offlow by varying vacuum battery 20 volume or number of vacuum lung pairs14. FIG. 7A is a plot showing flow volume vs. time, and FIG. 7B is aplot showing battery volume vs. time needed to load. FIG. 7A and FIG. 7Billustrate fine tuning by varying the stored vacuum potential via changein vacuum battery volume. Time gap out of vacuum was 10 min, with n=3.The auxiliary vacuum battery 30 was kept constant at 100 μl, while themain vacuum battery 20 volume was carried. Aside from increasing flowreliability and speed, it was found out that the larger the battery, thefaster the flow rate. However, there was a saturation of flow rate afterthe battery was larger than 150 μl. Little difference was found inloading times between the 150 μl and 200 μl battery. The simulationresults (described in further detail below) were plotted with dashedlines, and agreed well with experimental results that were in dots.

In sum, it was found that the loading time was inversely proportional tothe volume of the vacuum battery, and reaches saturation as the volumegets larger. We were able to tune the flow rates at finer incrementsfrom about 9.0 μl/min to about 16.7 μl/min. It was possible to easilytune flow rates by simply punching different diameter sizes for thevacuum void 20 after the mold was already fabricated.

Next, the effect of vacuum lung cross-section area on flowcharacteristics was tested. Coarse tuning may be accomplished by varyingthe diffusion surface area as a result of changing the number of lungpairs 14.

Referring to FIG. 8A and FIG. 8B, showing close-up images of an 8-lungpair 14A and 4-lung pair 14 b respectively, the gas exchange of the lungalveoli are mimicked by closely staggered fluid channels 26 a/26 b andvacuum channels 24 a/24 b in an array where a 300 μm thin PDMS membraneseparates them. A “lung pair” is defined as one fluid channel 26 a/26 bplus one vacuum channel 24 a/24 b.

As illustrated in FIG. 8A and FIG. 8B, the fluid and vacuum channels donot physically connect with each other, as all pressure differences areactuated by gas diffusion across the thin PDMS wall. This is similar tothe concept that blood vessels do not connect with the atmosphericenvironment in alveoli, but rely on diffusion for gas exchange. Both thefluid channels 26 a/26 b and vacuum channels 24 a/24 b were sized at 300μm in width and height, and 16.8 mm in length. Each lung pair was sizedhaving a 10 mm² diffusion cross section area. It is appreciated thatother sizing and geometry may be contemplated.

FIG. 9A shows a plot of flow volume vs. time for varying numbers of lungpairs. FIG. 9B shows a plot of loading time vs. numbers of lung pairs.FIG. 9A and FIG. 9B show that the number of lung pairs, which determinesthe diffusion cross section, is proportional to the flow speed, andloading time was also inversely proportional to the surface area of thediffusion cross-section area. It was possible to tune flow rates with alarger range from about 1.6 to about 18.2 μl/min by adding the number of“lung pairs.” The vacuum lungs 14 had a more dramatic effect ofincreasing loading speed up to 10 times compared to chips that did nothave any vacuum lungs. In order to tune flow rates, the mold has to bepredesigned with the desired number of lung pairs.

Referring to FIG. 10 and FIG. 11, flow rate decay measurements were alsoconducted and showed constant flow rates with slower decay with thevacuum battery system 10 than conventional degas pumping systems. FIG.10 is a plot of flow rate vs. elapsed time after loading for variouslung pair quantities and bulk degassing, and shows that flow rates decayslower with the vacuum battery system 10 when there are more lung pairs.The time gap out of vacuum was 15 min. FIG. 11 is a plot of the timeconstant of flow rate for various lung pair quantities and bulkdegassing, and shows the exponential decay time constant is 5 timesslower with the vacuum battery system 10 compared to conventional degaspumping. Both vacuum batteries were kept constant at 100 μl for allexperiments, n=3.

FIG. 12 through FIG. 14 show results from quantitative digital detectionof HIV RNA from human blood using the vacuum battery system 10 of thepresent disclosure. Isothermal nucleic acid amplification with therecombinase polymerase amplification (RPA) chemistry is demonstrated onsystem 10. The chip 12 first compartmentalizes the blood sample into 224wells 28 for digital amplification. RPA reagents are lyophilized in thewells. After compartmentalization, the user places the chip on aninstant heat pack and incubates for at least 30 minutes, then an endpoint fluorescent count is taken of how many wells show positive. FIG.12A through FIG. 12F show actual fluorescent images of the reactions(contrast adjusted) and the correlation with nucleic acid concentration.FIG. 13 is a plot of the average intensity of time, showing that theintensity of positive spots increases to a detectable level in 10minutes. FIG. 14 is a pot showing the detection range of the system 10.MRSA DNA was spiked into human whole blood for these tests.

Referring to the plots of FIG. 17A (showing number of wells digitizedover time) and FIG. 17B (showing the time needed to load all wells forvarious battery volumes), the time needed to load all the wells wasshowed to decrease on increasing battery volume. Furthermore, loadingand compartmentalization of all wells was completed in 12 minutes withthe vacuum battery system 10 (solid line in FIG. 17B), whereasconventional degassing well loading took 23 minutes (dashed line in FIG.17B).

The digitization speed of the wells 28 was also characterized by varyingthe loading time gap, as illustrated in the plots of FIG. 18A and FIG.18B, demonstrating about 2 times faster dead-end loading compared toconventional degas pumping.

Referring now to FIG. 15, a simplified 2-D diffusion model was builtwith the COMSOL simulation software using the convection diffusionequation. The vacuum battery system 10 was simplified into a 2D modelwith four regions, from left to right, the fluid channel 16 where air isbeing drawn out, the thin PDMS membrane (between channels 24 and 26) ofthe vacuum lungs 14 to control diffusion speed, the vacuum battery voidspace 20 to store vacuum potential, and the surrounding bulk PDMSmaterial. Within the PDMS regions, it assumed that there was noconvection. Air diffuses gradually from the left to right regions.

The above experiments also demonstrated that it was possible to designwide fluidic channels (e.g. 3×15 mm, 300 μm height) in the chip 12 andload without any bubbles, which has been previously difficult to performin capillary or plastic microfluidic systems, where trapping of bubblesis a common problem in wider geometries. It is critical to minimizebubbles in microfluidic systems, as they can easily clog channels, orcause catastrophic ejection of liquid when heated due to thermalexpansion. This is a particular problem in PCR assays.

FIG. 16 shows the simulated pressure profile of the dashed line in FIG.15. As time increases, the vacuum battery void space 20 first fills withair, then it gradually diffuses into the bulk PDMS. The bulk PDMSdegassing follows a characteristic exponential decay in pressure.

The air diffusion across from the fluid channels through the PDMS vacuumlungs into the vacuum battery space can be described with theconvection-diffusion equation:

$\begin{matrix}{\frac{\partial c_{i}}{\partial t} = {{\nabla{\cdot \left( {D_{i}{\nabla c_{i}}} \right)}} - {\nabla{\cdot \left( {\overset{\rightarrow}{u}c_{i}} \right)}}}} & {{Eq}.\mspace{14mu} 1}\end{matrix}$

where c_(i) denotes the concentration species of air in the fluidchannel, PDMS, or vacuum battery. D_(i) is the diffusion constant of airin each regime, and {right arrow over (u)} is the convection velocityvector in the fluid channel and vacuum battery. In the bulk PDMS, thereis no convection, therefore the equation simplifies into Fick's secondlaw:

$\begin{matrix}{\frac{\partial c_{i}}{\partial t} = {D{\nabla^{2}c_{i}}}} & {{Eq}.\mspace{14mu} 2}\end{matrix}$

The pressure in the fluid channels and vacuum battery can be found bycorrelating the gas concentration via the ideal gas law:

$\begin{matrix}{P = {{\frac{n}{V}{RT}} = {cRT}}} & {{Eq}.\mspace{14mu} 3}\end{matrix}$

where P is the pressure, V is the volume, n is number of moles, R is theAvogadro number, and T is the temperature. The volume of liquid beingsucked in the device is the same volume of air that has diffused intothe vacuum battery and PDMS. This volume can be calculated byintegrating the flux of air concentration being degassed over time andsurface area. Pressure changes against time plots are shown in FIG. 16.

In conclusion, the battery vacuum system and methods of the presentdisclosure provide significant advantages over conventional degaspumping via extended (about 2 hrs) and reliable flow (about 8 times lessstandard deviation in loading time). Loading speed was easily tuned andenhanced up to 10 times by varying the diffusion area of vacuum lungs orchanging the size of the vacuum void. In one exemplary configuration,the pumping mechanism of the battery vacuum system is capable of loadingat least 140 μl of liquid, and compartmentalizing liquids into hundredsof dead-end wells for digital amplification or multiplexed assayapplications.

Since the vacuum battery chips 12 can be easily integrated intooptically clear microfluidic circuits while leaving design flexibilityfor different geometry, they are particularly advantageous applicationsusing controlled pumping in low cost power-free handheld devices. Thevacuum battery system 10 is also particularly useful in point-of-carediagnostics, as the system is robust and requires no technical skill orextra peripheral equipment/power sources for operation. As ademonstration of its utility, the vacuum battery system was integratedwith isothermal digital nucleic acid amplification and sample prep forquantitative detection of Methicillin-Resistant Staphylococcus Aureus(MRSA) DNA directly from human blood samples.

It was shown that the vacuum batteries and vacuum lungs of the presentdescription contributed to more consistent flow rates, as the slope ofloading was more linear. It was also shown that the vacuum lungsincrease not only the loading speed, but also the flow stability. Flowrate followed the characteristic exponential decay over time as inconventional degas pumping, however, the flow rate decay could be mademuch slower when there are more lung pairs. We were able to increase theexponential decay time constant about 5 times with this prototype. Weanticipate that is it possible to further optimize the vacuum batterysystem to make the decay time constant even longer by adding extravacuum batteries and additional secondary degas lungs to degas andstabilize the primary vacuum battery.

The vacuum battery system was integrated with a digital plasmaseparation system that is capable of separating plasma via “microcliffstructures” into hundreds to thousands of nano-liter scale wells toperform digital amplification. Different spiked DNA concentrations weretested using an isothermal nucleic acid amplification technique calledRecombinase Polymerase Amplifcation (RPA). Quantitative detection ofMRSA DNA from about 10 to about 10⁵ copies/μl directly from spiked humanwhole blood was achieved.

The vacuum battery system also demonstrated loading of a large array ofdead-end wells (224 in total) without trapping any bubbles up to 2 timesfaster. These dead-end wells may be implemented in multiplexed assays ordigital PCR assays. Faster bubble-free loading of large optical windowsand deep wells were shown, which are useful in transmission type opticaldetection. The vacuum battery system does not require any specialsurface treatment and has more flexibility for channel geometry design,as it does not rely on surface tension or capillary action to driveflow.

The attributes of the vacuum battery system may also be tuned accordingto one or more of the following: (1) increase the vacuum battery void iflonger operation time or sample volume is needed; (2) increase thenumber of vacuum lung pairs if faster flow speed is desired, (3)increase the waste reservoir volume if larger sample volumes arenecessary.

Furthermore, pumping components of the system may be directly integratedinto the chip 12 and can be easily manufactured by molding. For massproduction, PDMS can be replaced by the use of injection moldingcompatible gas permeable elastomers (e.g. liquid silicone, TPE, etc.).In one embodiment, the chip construction only uses two layers, thus itcan be manufactured at low cost. Furthermore, flow rate can be furtherstabilized by adding second order vacuum battery systems to degas themain battery system 18.

In summary, compared to conventional degas loading, the vacuum batterysystem provides significantly more reliable flow, longer operationaltime, faster flow, and easy tunablity of flow rates. In addition, itovercomes several limitations of capillary loading. The vacuum batterysystem is able to load dead-end wells, load deep or wide geometrieswithout bubbles, and has excellent transparent optical properties. Thissimple system is easy to operate, can be stored for long term, isconvenient to transport, and can be operated on-site without anyexternal power sources or equipment. This translates into numerousapplications, such as performing on-site ELISA, digital PCR, ormultiplexed digital nucleic acid amplification.

For at least these reasons, the vacuum battery system 10 provides anideal alternative platform technology from capillary systems orconventional degas pumping for handheld point-of-care devices.

From the description herein, it will be appreciated that that thepresent disclosure encompasses multiple embodiments which include, butare not limited to, the following:

1. A system for portable fluidic pumping, the system comprising: a chip;a void disposed within the chip; the void comprising a volume configuredto store a vacuum upon subjecting the chip to a vacuum state; a vacuumchannel coupled to and in communication with the void; a fluid channeldisposed adjacent to the vacuum channel such that a thin gas-permeablewall of material is disposed between the fluid channel and the vacuumchannel; wherein the fluid channel and vacuum channel are not physicallyconnected to each other; and a containment for maintaining the chip insaid vacuum state; wherein upon release of the chip from the vacuumstate in the containment, the stored vacuum within the void passivelydraws air across the thin gas-permeable wall into the void to advance afluid sample into the fluid channel.

2. The system of any preceding embodiment: wherein the vacuum channelcomprises a plurality of vacuum channels and the fluid channel comprisesa plurality of fluid channels; and wherein the vacuum channels areinter-digitated with the plurality of fluid channels to form a vacuumlung of thin gas-permeable walls.

3. The system of any preceding embodiment, wherein the vacuum lung isconfigured to mimic lung alveoli gas exchange by allowing air to diffuseacross the thin gas-permeable walls between the fluid channels and thevacuum channels and void.

4. The system of any preceding embodiment, wherein the lung isconfigured to control gas diffusion across the thin gas-permeable walls,thereby regulating flow properties of fluid in the fluid channels.

5. The system of any preceding embodiment: wherein the fluid channelfurther comprises a plurality of dead-end wells coupled in series; andwherein the fluid sample is configured to be sequentially drawn into theplurality of dead-end wells.

6. The system of any preceding embodiment, further comprising: aplurality of auxiliary vacuum channels inter-digitated with theplurality of dead end wells to form a second set of thin gas-permeablewalls between the dead-end wells and auxiliary vacuum channels; andwherein upon release of the chip from the vacuum state, air is drawnacross the second set of thin gas-permeable walls to advance the fluidsample into the plurality of dead-end wells.

7. The system of any preceding embodiment, further comprising: anauxiliary void coupled to the auxiliary vacuum channels; the auxiliaryvoid comprising a volume configured to store a vacuum upon subjectingthe chip to a vacuum state; wherein upon release of the chip from thevacuum state, the stored vacuum within the auxiliary void draws airacross the second set of thin gas-permeable walls to advance the intothe plurality of dead-end wells.

8. The system of any preceding embodiment, further comprising: areservoir coupled to the fluid channel; wherein upon release of the chipfrom the vacuum state, fluid is advanced from the inlet into thereservoir along the fluid channel.

9. The system of any preceding embodiment, further comprising: areservoir coupled to the fluid channel; and an inlet disposed in thechip; the inlet being coupled to and in communication with the fluidchannel and configured to receive a sample fluid; wherein upon releaseof the chip from the vacuum state, fluid is advanced from the inlet andsequentially through the plurality of dead-end wells, the reservoir, andthen the plurality of fluid channels.

10. The system of any preceding embodiment, wherein the chip comprises:a first layer of gas-permeable material; the first layer comprising oneor more of the vacuum channel, fluid channel, and void; and a secondlayer capping the first layer to close off one or more of the vacuumchannel, fluid channel, and void.

11. The system of any preceding embodiment: wherein the chip comprisesmultiple layers; and wherein one or more of the vacuum channel, fluidchannel, and void are disposed on separate layers.

12. A method for portable fluidic pumping on a chip, the systemcomprising: providing a chip comprising a void, a vacuum channel and afluid channel disposed within the chip, wherein the vacuum channel iscoupled to and in communication with the void and the fluid channel isdisposed adjacent to the vacuum channel such that a thin gas-permeablewall of material is disposed between the fluid channel and the vacuumchannel; applying a vacuum to the chip to charge the chip to store avacuum within the void; storing the chip to maintain the vacuum;discharging the chip from the vacuum; applying a fluid sample at alocation on the chip; and as a result of the stored vacuum within thevoid, passively drawing air across the thin gas-permeable wall into thevoid to advance the fluid sample into the fluid channel.

13. The method of any preceding embodiment, wherein storing the chip tomaintain the vacuum comprises placing the chip in a vacuum-sealed pouch.

14. The method of any preceding embodiment, wherein discharging the chipcomprises opening the vacuum-sealed pouch to break the vacuum.

15. The method of any preceding embodiment: wherein the vacuum channelcomprises a plurality of vacuum channels and the fluid channel comprisesa plurality of fluid channels; and wherein the plurality of vacuumchannels are inter-digitated with the plurality of fluid channels toform a vacuum lung of thin gas-permeable walls.

16. The method of any preceding embodiment, further comprising the stepof: controlling gas diffusion across the gas-permeable walls to regulatea rate of flow of the sample fluid into the fluid channels.

17. The method of any preceding embodiment: wherein the fluid channelcomprises a plurality of dead-end wells; and wherein the method furthercomprises sequentially drawing the fluid sample into the plurality ofdead-end wells.

18. The method of any preceding embodiment: wherein the fluid channelfurther comprises a reservoir; and wherein advancing the fluid samplecomprises advancing the fluid sample from the location to the fluidchannel and reservoir.

19. The method of any preceding embodiment: wherein the fluid channelfurther comprises a reservoir; wherein the location comprises an inletto the fluid channel; and wherein advancing the fluid sample comprisesadvancing the fluid sample from the inlet sequentially into theplurality of dead-end wells, the reservoir, and then into the pluralityof fluid channels.

20. The method of any preceding embodiment, wherein storing the chip tomaintain the vacuum comprises storing the chip for at least a day priorto release of the chip from the vacuum state.

21. A portable device for pumping a fluid sample, comprising: a chipcomprising a plurality of vacuum channels and a plurality of fluidchannels; a vacuum battery void disposed within the chip; the vacuumbattery void comprising a volume configured to store a vacuum uponsubjecting the chip to a vacuum state; wherein the plurality of vacuumchannels are adjacent with the plurality of fluid channels to form avacuum lung of thin gas-permeable walls disposed between the pluralityof vacuum channels and plurality of fluid channels; wherein theplurality of vacuum channels are coupled to and in communication withthe vacuum battery void; wherein the plurality of vacuum channels andplurality of spaced apart fluid channels are not physically connected toeach other; and wherein upon release of the chip from the vacuum state,the stored vacuum within the vacuum battery void passively draws airacross the thin gas-permeable walls into the vacuum battery void toadvance the fluid sample into the plurality of spaced apart fluidchannels.

22. The portable device of any preceding embodiment, wherein the vacuumlung is configured to mimic lung alveoli gas exchange by allowing air todiffuse through the thin gas permeable walls across the fluid channelsand the vacuum channels and vacuum battery void.

23. The portable device of any preceding embodiment, wherein the lung isconfigured to control gas diffusion across the gas-permeable walls,thereby regulating flow properties of fluid in the plurality of fluidchannels.

24. The portable device of any preceding embodiment, further comprising:a plurality of dead-end wells coupled to the plurality of fluidchannels; wherein the fluid sample is configured to be sequentiallydrawn into the plurality of dead-end wells.

25. The portable device of any preceding embodiment, further comprising:a plurality of auxiliary vacuum channels inter-digitated with theplurality of dead end wells to for a second set of thin gas-permeablewalls between the dead-end wells and auxiliary vacuum channels; andwherein upon release of the chip from the vacuum state, air is drawnacross the second set of thin gas-permeable walls to advance the intothe plurality of dead-end wells.

26. The portable device of any preceding embodiment, further comprising:an auxiliary vacuum battery void coupled to the auxiliary vacuumchannels; the auxiliary vacuum battery void comprising a volumeconfigured to store a vacuum upon subjecting the chip to a vacuum state;wherein upon release of the chip from the vacuum state, the storedvacuum within the auxiliary vacuum battery void draws air across thesecond set of thin gas-permeable walls to advance the fluid sample intothe plurality of dead-end wells.

27. The portable device of any preceding embodiment, further comprising:a reservoir coupled to the plurality of fluid channels; wherein uponrelease of the chip from the vacuum state, the fluid sample is advancedfrom the plurality of fluid channels and into the reservoir.

28. The portable device of any preceding embodiment: wherein the chipfurther comprises a reservoir and an inlet coupled to the plurality offluid channels, the inlet disposed at a location on the chip; andwherein upon release of the chip from the vacuum state, the fluid sampleis sequentially advanced from the inlet into the plurality of dead-endwells, into the reservoir, and then into the plurality of fluidchannels.

29. The portable device of any preceding embodiment, wherein the chipcomprises: a first layer of gas-permeable material; the first layercomprising one or more of the plurality of vacuum channels, plurality offluid channels, and battery vacuum void; and a second layer capping thefirst layer to close off one or more of the plurality of vacuumchannels, plurality of fluid channels, and battery vacuum void.

30. The portable device of any preceding embodiment: wherein the chipcomprises multiple layers; and wherein one or more of the vacuumchannels, fluid channels, and battery vacuum void are disposed onseparate layers.

31. The portable device of any preceding embodiment, further comprising;a pair of non-permeable layers coupled to top and bottom surfaces of thechip.

32. The portable device of any preceding embodiment, further comprisinga containment for maintaining the chip in said vacuum state prior torelease of said vacuum state.

Although the description herein contains many details, these should notbe construed as limiting the scope of the disclosure but as merelyproviding illustrations of some of the presently preferred embodiments.Therefore, it will be appreciated that the scope of the disclosure fullyencompasses other embodiments which may become obvious to those skilledin the art.

In the claims, reference to an element in the singular is not intendedto mean “one and only one” unless explicitly so stated, but rather “oneor more.” All structural, chemical, and functional equivalents to theelements of the disclosed embodiments that are known to those ofordinary skill in the art are expressly incorporated herein by referenceand are intended to be encompassed by the present claims. Furthermore,no element, component, or method step in the present disclosure isintended to be dedicated to the public regardless of whether theelement, component, or method step is explicitly recited in the claims.No claim element herein is to be construed as a “means plus function”element unless the element is expressly recited using the phrase “meansfor”. No claim element herein is to be construed as a “step plusfunction” element unless the element is expressly recited using thephrase “step for”.

What is claimed is:
 1. A system for portable fluidic pumping, the systemcomprising: a chip; a void disposed within the chip; the void comprisinga volume configured to store a vacuum upon subjecting the chip to avacuum state; a vacuum channel coupled to and in communication with thevoid; a fluid channel disposed adjacent to the vacuum channel such thata thin gas-permeable wall of material is disposed between the fluidchannel and the vacuum channel; wherein the fluid channel and vacuumchannel are not physically connected to each other; and a containmentfor maintaining the chip in said vacuum state; wherein upon release ofthe chip from the vacuum state in the containment, the stored vacuumwithin the void passively draws air across the thin gas-permeable wallinto the void to advance a fluid sample into the fluid channel.
 2. Asystem as recited in claim 1: wherein the vacuum channel comprises aplurality of vacuum channels and the fluid channel comprises a pluralityof fluid channels; and wherein the vacuum channels are inter-digitatedwith the plurality of fluid channels to form a vacuum lung of thingas-permeable walls.
 3. A system as recited in claim 2, wherein thevacuum lung is configured to mimic lung alveoli gas exchange by allowingair to diffuse across the thin gas-permeable walls between the fluidchannels and the vacuum channels and void.
 4. A system as recited inclaim 2, wherein the lung is configured to control gas diffusion acrossthe thin gas-permeable walls, thereby regulating flow properties offluid in the fluid channels.
 5. A system as recited in claim 2: whereinthe fluid channel further comprises a plurality of dead-end wellscoupled in series; and wherein the fluid sample is configured to besequentially drawn into the plurality of dead-end wells.
 6. A system asrecited in claim 5, further comprising: a plurality of auxiliary vacuumchannels inter-digitated with the plurality of dead end wells to form asecond set of thin gas-permeable walls between the dead-end wells andauxiliary vacuum channels; and wherein upon release of the chip from thevacuum state, air is drawn across the second set of thin gas-permeablewalls to advance the fluid sample into the plurality of dead-end wells.7. A system as recited in claim 6, further comprising: an auxiliary voidcoupled to the auxiliary vacuum channels; the auxiliary void comprisinga volume configured to store a vacuum upon subjecting the chip to avacuum state; wherein upon release of the chip from the vacuum state,the stored vacuum within the auxiliary void draws air across the secondset of thin gas-permeable walls to advance the fluid sample into theplurality of dead-end wells.
 8. A system as recited in claim 1, furthercomprising: a reservoir coupled to the fluid channel; wherein uponrelease of the chip from the vacuum state, fluid is advanced from thefluid channel into the reservoir along the fluid channel.
 9. A system asrecited in claim 5, further comprising: a reservoir coupled to the fluidchannel; and an inlet disposed in the chip; the inlet being coupled toand in communication with the fluid channel and configured to receive asample fluid; wherein upon release of the chip from the vacuum state,fluid is advanced from the inlet and sequentially through the pluralityof dead-end wells, the reservoir, and then the plurality of fluidchannels.
 10. A system as recited in claim 1, wherein the chipcomprises: a first layer of gas-permeable material; the first layercomprising one or more of the vacuum channel, fluid channel, and void;and a second layer capping the first layer to close off one or more ofthe vacuum channel, fluid channel, and void.
 11. A system as recited inclaim 1: wherein the chip comprises multiple layers; and wherein one ormore of the vacuum channel, fluid channel, and void are disposed onseparate layers.
 12. A method for portable fluidic pumping on a chip,the system comprising: providing a chip comprising a void, a vacuumchannel and a fluid channel disposed within the chip, wherein the vacuumchannel is coupled to and in communication with the void and the fluidchannel is disposed adjacent to the vacuum channel such that a thingas-permeable wall of material is disposed between the fluid channel andthe vacuum channel; applying a vacuum to the chip to charge the chip tostore a vacuum within the void; storing the chip to maintain the vacuum;discharging the chip from the vacuum; applying a fluid sample at alocation on the chip; and as a result of the stored vacuum within thevoid, passively drawing air across the thin gas-permeable wall into thevoid to advance the fluid sample into the fluid channel.
 13. A method asrecited in claim 12, wherein storing the chip to maintain the vacuumcomprises placing the chip in a vacuum-sealed pouch.
 14. A method asrecited in claim 13, wherein discharging the chip comprises opening thevacuum-sealed pouch to break the vacuum.
 15. A method as recited inclaim 12: wherein the vacuum channel comprises a plurality of vacuumchannels and the fluid channel comprises a plurality of fluid channels;and wherein the plurality of vacuum channels are inter-digitated withthe plurality of fluid channels to form a vacuum lung of thingas-permeable walls.
 16. A method as recited in claim 15, furthercomprising the step of: controlling gas diffusion across thegas-permeable walls to regulate a rate of flow of the sample fluid intothe fluid channels.
 17. A method as recited in claim 15: wherein thefluid channel comprises a plurality of dead-end wells; and wherein themethod further comprises sequentially drawing the fluid sample into theplurality of dead-end wells.
 18. A method as recited in claim 12:wherein the fluid channel further comprises a reservoir; and whereinadvancing the fluid sample comprises advancing the fluid sample from thelocation to the fluid channel and reservoir.
 19. A method as recited inclaim 17: wherein the fluid channel further comprises a reservoir;wherein the location comprises an inlet to the fluid channel; andwherein advancing the fluid sample comprises advancing the fluid samplefrom the inlet sequentially into the plurality of dead-end wells, thereservoir, and then into the plurality of fluid channels.
 20. A methodas recited in claim 12, wherein storing the chip to maintain the vacuumcomprises storing the chip for at least a day prior to release of thechip from the vacuum state.
 21. A portable device for pumping a fluidsample, comprising: a chip comprising a plurality of vacuum channels anda plurality of fluid channels; a vacuum battery void disposed within thechip; the vacuum battery void comprising a volume configured to store avacuum upon subjecting the chip to a vacuum state; wherein the pluralityof vacuum channels are adjacent with the plurality of fluid channels toform a vacuum lung of thin gas-permeable walls disposed between theplurality of vacuum channels and plurality of fluid channels; whereinthe plurality of vacuum channels are coupled to and in communicationwith the vacuum battery void; wherein the plurality of vacuum channelsand plurality of spaced apart fluid channels are not physicallyconnected to each other; and wherein upon release of the chip from thevacuum state, the stored vacuum within the vacuum battery void passivelydraws air across the thin gas-permeable walls into the vacuum batteryvoid to advance the fluid sample into the plurality of spaced apartfluid channels.
 22. A portable device as recited in claim 21, whereinthe vacuum lung is configured to mimic lung alveoli gas exchange byallowing air to diffuse through the thin gas permeable walls across thefluid channels and the vacuum channels and vacuum battery void.
 23. Aportable device as recited in claim 22, wherein the lung is configuredto control gas diffusion across the gas-permeable walls, therebyregulating flow properties of fluid in the plurality of fluid channels.24. A portable device as recited in claim 21, further comprising: aplurality of dead-end wells coupled to the plurality of fluid channels;wherein the fluid sample is configured to be sequentially drawn into theplurality of dead-end wells.
 25. A portable device as recited in claim24, further comprising: a plurality of auxiliary vacuum channelsinter-digitated with the plurality of dead end wells to for a second setof thin gas-permeable walls between the dead-end wells and auxiliaryvacuum channels; and wherein upon release of the chip from the vacuumstate, air is drawn across the second set of thin gas-permeable walls toadvance the into the plurality of dead-end wells.
 26. A portable deviceas recited in claim 25, further comprising: an auxiliary vacuum batteryvoid coupled to the auxiliary vacuum channels; the auxiliary vacuumbattery void comprising a volume configured to store a vacuum uponsubjecting the chip to a vacuum state; wherein upon release of the chipfrom the vacuum state, the stored vacuum within the auxiliary vacuumbattery void draws air across the second set of thin gas-permeable wallsto advance the fluid sample into the plurality of dead-end wells.
 27. Aportable device as recited in claim 21, further comprising: a reservoircoupled to the plurality of fluid channels; wherein upon release of thechip from the vacuum state, the fluid sample is advanced from theplurality of fluid channels and into the reservoir.
 28. A portabledevice as recited in claim 24: wherein the chip further comprises areservoir and an inlet coupled to the plurality of fluid channels, theinlet disposed at a location on the chip; and wherein upon release ofthe chip from the vacuum state, the fluid sample is sequentiallyadvanced from the inlet into the plurality of dead-end wells, into thereservoir, and then into the plurality of fluid channels.
 29. A portabledevice as recited in claim 21, wherein the chip comprises: a first layerof gas-permeable material; the first layer comprising one or more of theplurality of vacuum channels, plurality of fluid channels, and batteryvacuum void; and a second layer capping the first layer to close off oneor more of the plurality of vacuum channels, plurality of fluidchannels, and battery vacuum void.
 30. A portable device as recited inclaim 21: wherein the chip comprises multiple layers; and wherein one ormore of the vacuum channels, fluid channels, and battery vacuum void aredisposed on separate layers.
 31. A portable device as recited in claim21, further comprising; a pair of non-permeable layers coupled to topand bottom surfaces of the chip.
 32. A portable device as recited inclaim 21, further comprising a containment for maintaining the chip insaid vacuum state prior to release of said vacuum state.